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Tunable Atomic-Scale Steps and Cavities Break Both Stability and Activity Limits of CoO_(x) Nanosheets to Catalyze Oxygen Evolution

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Renewables 2023年第4期1卷 465-473页

作者： Min Yu Xueqin Mu Weitao Meng Ziyue Chen Yu Tong Yu Ge Shiyuan Pang Shengjie Li Suli Liu Shichun Mu Key Laboratory of Advanced Functional Materials of Nanjing Nanjing Xiaozhuang UniversityNanjing 211171 State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan 430070

A highly active interface can enhance the catalytic efficiency of catalysts toward the oxygen evolution reaction(OER).However,accurately tuning their atomic interface configurations of defects with sufficient activity and stability remains a grand ***,we report on breaking the activity and stability limits of CoO_(x) nanosheets in the OER process by constructing copious high-energy atomic steps and cavities,in which S or Ce atoms simultaneously replace O or Co atoms from CoO_(x),thus achieving high-energy atomic interface Ce,O-Co_(3)S_(4) *** combining in situ characterization and density functional theory calculations,it is shown that the unique orbital coupling between Ce-4f,O(S)-2p,and Co-3d causes it to be closer to the Fermi level,leading to faster charge transfer *** importantly,the novel structure breaks the stability limit of cobalt sulfide with planar defects,which gives high catalytic activity and stability in 0.1 M KOH solutions,better than commercial RuO_(2) and IrO_(2) noble metal *** expected,Ce,O-Co_(3)S_(4) possesses much better turnover frequency activity(0.064 s^(-1))at an overpotential of 300 mV,which is ~7 times larger than that of Ce-CoO_(x)(0.009 s^(-1)).Our work presents a new perspective of designing catalysts with atomically dispersed orbital electronic coupling defects toward efficient OER electrocatalysis.

关键词： atomic replacement amorphous structures interface active centers atomic defect oxygen evolution reaction

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具有分级界面的纳米纤维增强聚合物复合材料:用于高温介电储能应用

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Science China materials 2023年第7期66卷 2652-2661页

作者：智佳鹏王建沈忠慧李宝文张鑫南策文 State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Center of Smart Materials and Devices&International School of Materials Science and EngineeringWuhan University of TechnologyWuhan 430070China School of Materials Science and Engineering State Key Lab of New Ceramics and Fine ProcessingTsinghua UniversityBeijing 100084China

陶瓷纳米填料增强的柔性聚合物基复合材料在先进电子电气系统中显示出巨大的储能应用潜力.但如何在高于150℃的条件下提高其能量密度和效率仍然是一个挑战.本文中我们采用氮化硼-钛酸钡(BNBaTiO_(3))非均质纳米纤维作为填料,耐高温的聚... 详细信息

陶瓷纳米填料增强的柔性聚合物基复合材料在先进电子电气系统中显示出巨大的储能应用潜力.但如何在高于150℃的条件下提高其能量密度和效率仍然是一个挑战.本文中我们采用氮化硼-钛酸钡(BNBaTiO_(3))非均质纳米纤维作为填料,耐高温的聚醚酰亚胺(PEI)为基体,使复合材料的介电常数和击穿强度同时提高.分级结构的BN/BaTiO_(3)/PEI界面提升了材料的陷阱密度和能级,可进一步抑制传导损耗.在此基础上,复合材料在150℃,能量效率高于90%时展现出5.23J cm^(-3)的超高能量密度,这是迄今为止纳米纤维增强聚合物复合材料中最高的能量密度.研究表明,分级界面是提高材料高温储能的有效策略,对介电材料在高温下的应用具有重要意义.

关键词： high temperature energy storage dielectrics polymer nanocomposite film capacitor

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Boosting molecular diffusion following the generalized Murray's Law by constructing hierarchical zeolites for maximized catalytic activity

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国家科学评论（英文版） 2022年第12期9卷 143-156页

作者： Ming-Hui Sun Shu-Shu Gao Zhi-Yi Hu Tarek Barakat Zhan Liu Shen Yu Jia-Min Lyu Yu Li Shu-Tao Xu Li-Hua Chen Bao-Lian Su State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan 430070China Laboratory of Inorganic Materials Chemistry(CMI) University of NamurNamur B-5000Belgium Division of Analysis Sinopec Beijing Research Institute of Chemical IndustryBeijing 100013China National Engineering Laboratory for Methanol to Olefins Dalian National Laboratory for Clean EnergyDalian Institute of Chemical PhysicsChinese Academy of SciencesDalian 116023China State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan 430070China Nanostructure Research Centre Wuhan University of TechnologyWuhan 430070China Laboratory of Inorganic Materials Chemistry(CMI) University of NamurNamur B-5000Belgium State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan 430070China National Engineering Laboratory for Methanol to Olefins Dalian National Laboratory for Clean EnergyDalian Institute of Chemical PhysicsChinese Academy of SciencesDalian 116023China

Diffusion is an extremely critical step in zeolite catalysis that determines the catalytic performance,in particular for the conversion of bulky *** interconnected mesopores and macropores into a single microporous zeolite with the rationalized pore size at each level is an effective strategy to suppress the diffusion limitations,but remains highly challenging due to the lack of rational design ***,we demonstrate the first example of boosting molecular diffusion by constructing hierarchical Murray zeolites with a highly ordered and fully interconnected macro-meso-microporous structure on the basis of the generalized Murray's *** a hierarchical Murray zeolite with a refined quantitative relationship between the pore size at each length scale exhibited 9 and 5 times higher effective diffusion rates,leading to 2.5 and 1.5 times higher catalytic performance in the bulky 1,3,5-triisopropylbenzene cracking reaction than those of microporous ZSM-5 and ZSM-5 nanocrystals,*** concept of hierarchical Murray zeolites with optimized structural features and their design principles could be applied to other catalytic reactions for maximized performance.

关键词： catalytic cracking generalized Murray's Law hierarchical Murray structure ordered porous hierarchy zeolites

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Wet-milling synthesis of immobilized Pt/Ir nanoclusters as promising heterogeneous catalysts

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Nano Research 2022年第4期15卷 3065-3072页

作者： Peng Du Kai Huang Xiaoyuan Fan Jingteng Ma Naveed Hussain Ruyue Wang Bohan Deng Binghui Ge Haolin Tang Ru Zhang Ming Lei Hui Wu State Key Laboratory of Information Photonics and Optical Communications&School of Science Beijing University of Posts and TelecommunicationsBeijing 100876China State Key Laboratory of New Ceramics and Fine Processing School of Materials Science and EngineeringTsinghua UniversityBeijing 100084China Institute of Fundamental and Frontier Sciences University of Electronic Science and Technology of ChinaChengdu 610054China Institutes of Physical Science and Information Technology Anhui UniversityHefei 230601China State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan 430070China

Being a typical state of the art heterogeneous catalyst,supported noble metal catalyst often demonstrates enhanced catalytic ***,a facile synthetic method for realizing large-scale and low-cost supported noble metal catalyst is strictly *** this end,by making use of the strong metal-support interaction(SMSI)and mechanochemical reaction,we introduce an efficient synthetic route to obtain ultrafine Pt and Ir nanoclusters immobilized on diverse substrates by wet chemical *** further demonstrate the scaling-up effect of our approach by large-scale ball-milling production of Pt nanoclusters immobilized on TiO_(2)*** synthesized Pt/Ir@Co_(3)O_(4)catalysts exhibit superior oxygen evolution reaction(OER)performance with only 230 and 290 mV overpotential to achieve current density of 10 and 100 mA·cm^(-2),beating the catalytic performance of Co_(3)O_(4)supported Pt or Ir clusters and commercial Ir/*** is envisioned that the present work strategically directs facile ways for fabricating supported noble metal heterogeneous catalysts.

关键词： heterogeneous catalysts metal clusters wet milling large-scale production strong metal–support interaction

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Rechargeable metal(Li, Na, Mg, Al)-sulfur batteries: materials and advances

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Journal of Energy Chemistry 2021年第10期30卷 104-134,I0004页

作者： Xue Liu Yan Li Xu Xu Liang Zhou Liqiang Mai State Key Laboratory of Advanced Technology for Materials Synthesis and Processing International School of Materials Science and EngineeringWuhan University of TechnologyWuhan 430070HubeiChina Foshan Xianhu Laboratory of the Advanced Energy Science and Technology Guangdong Laboratory Xianhu Hydrogen ValleyFoshan 528200GuangdongChina

Energy and environmental issues are becoming more and more severe and renewable energy storage technologies are vital to solve the *** metal(Li,Na,Mg,Al)-sulfur batteries with low-cost and earth-abundant elemental sulfur as the cathode are attracting more and more interest for electrical energy storage in recent ***-sulfur(Li-S),room-temperature sodium-sulfur(RT Na-S),magnesium-sulfur(Mg-S)and aluminum-sulfur(Al-S)batteries are the most prominent candidates among *** obvious obstacles are hampering the developments of metal-sulfur ***-S and Na-S batteries are encumbered mainly by anode dendrite issues,polysulfides shuttle and low conductivity of ***-S and Al-S batteries are short of suitable *** this review,relationships between various employed nanostructured materials and electrochemical performances of metal-sulfur batteries have been ***,the selections of suitable electrolytes,anode protection,separator modifications and prototype innovations are all crucial to the developments of metal-sulfur batteries and are discussed at the same ***,we give a review on the advances of Li-S,RT Na-S,Mg-S and Al-S batteries from the point of view of materials,and then focus on perspectives of their future developments.

关键词： Lithium sulfur batteries Sodium sulfur batteries Magnesium sulfur batteries Aluminum sulfur batteries Energy materials

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Interdisciplinary exploration between magnetism and thermoelectricity

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Science Bulletin 2022年第9期67卷 891-894,M0003页

作者： Cuncheng Li Wenyu Zhao Qingjie Zhang State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan 430070China

Thermoelectrics have important applications in power generation and refrigeration through the direct energy conversion between heat and *** performance of thermoelectric(TE)materials can be qualified by dimensionless figure of merit ZT=σa2/κ,whereσ,a andκare the electrical conductivity,Seebeck coefficient and thermal conductivity,respectively.

关键词： conductivity Seebeck electrical

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synthesis of highly sinterable MgO powders for IR transparent ceramics

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Ceramics International 2025年

作者： Zhi, Yongli Mei, Bingchu Li, Weiwei Cheng, Jing Luo, Peng State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology Wuhan430070 China Jianghuai Advance Technology Center Hefei230000 China

MgO transparent ceramics (TCS) have attracted great interests in the field of infrared window materials due to its wide transmission range, excellent thermal conductivity, and balanced mechanical properties. To date, research on MgO transparent ceramics predominantly relies on commercial MgO powders by spark plasma sintering (SPS). Herein, we report highly sinterable MgO powders synthesized by co-precipitation method, which exhibits pure phase and particle size of 75 nm. When sintered at 950 °C under 45 MPa for 2 h by hot pressed (HP) method, the transmittance of the MgO ceramic sample with the thickness of 2 mm achieved 76.9 % at 0.4 μm and 88.3 % at 5 μm. These optical properties are comparable to or even superior to MgO TCS produced through SPS method. This work shows that the MgO particles synthesized via the co-precipitation method are suitable for producing high optical quality of MgO infrared (IR) transparent ceramics. © 2025

关键词： Thermal conductivity

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CO_(2) adsorption and activation on p-block catalyst Ga_(2)O_(3)

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Science China materials 2025年第2期68卷 590-596页

作者： Zhizhuang Liu Xiaoxu Kuang Baowen Li Chenghua Sun Rong Tu Song Zhang Chaozhou Branch of Chemistry and Chemical Engineering Guangdong Laboratory Chaozhou 521000China School of Materials Science and Engineering Wuhan University of TechnologyWuhan 430070China Department of Chemistry and Biotechnology Swinburne University of TechnologyHawthornVictoria 3122Australia State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan 430070China

The fixation and conversion of CO_(2)frommedium-and high-temperature industrial exhaust gases arescientifically important and challenging tasks owing to theharsh conditions ***_(2)O_(3),a stable p-block compound,is surprisingly active in the thermal conversion of hot CO_(2)waste gas,but its underlying mechanism remains *** study,we investigated CO_(2)adsorption and activationacross 11 different Ga_(2)O_(3)-terminated faces using densityfunctional *** transfer and chemical bond analysesrevealed the occurrence of two distinct activation mechanismsinvolving synchronous electron gain and loss,driven by astrong synergetic effect between Ga cations and O anions onthe substrate *** Ga-O synergy enhances the CO_(2)activation efficiency compared with single active sites,with CO_(2)^(δ+) cation more readily capturing H atom than CO_(2)^(δ–).Tothe best of our knowledge,such a dual activation mechanismhas not been reported before,particularly for p-block *** findings provide new insights into the direct catalyticconversion of CO_(2)emissions and offer strategies for the rational design of industrial-grade catalysts for medium-andhigh-temperature CO_(2)tail gas conversion.

关键词： p-block catalyst gallium oxide carbon dioxide density functional theory synergetic mechanism

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Microstructures and mechanical properties of B4C–TiB2 ceramics fabricated by reactive sintering using B4C–Ti mixture

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Ceramics International 2025年

作者： Cui, Yi Bao, Sizhuo Sun, Yan Zhang, Ao He, Qianglong Wang, Weimin State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology Wuhan430070 China School of Materials Science and Engineering Wuhan University of Technology Wuhan430070 China

In this study, B4C–TiB2 ceramics were prepared via reactive sintering using B4C–Ti as the raw material. By investigating the sintering curve, microstructures, and mechanical properties at different sintering temperatures, the liquid-phase sintering environment provided by Ti melting was found to play a key role in densification. The high-speed densification stage occurs between 1800 and 1900 °C, which improves the comprehensive properties of B4C–TiB2 composite ceramics at 1900 °C. B4C–TiB2 composites achieved the best comprehensive properties at 1950 °C. Relative density, Vickers hardness, bending strength, and fracture toughness were 99.3 %, 32.6 GPa, 433 MPa, and 5.25 MPa m1/2, respectively. Vickers hardness and bending strength were affected by density, while fracture toughness was also affected by the TiB2 phase distribution. Additionally, improvement in fracture toughness was the result of the joint action of crack deflection, crack bridging, crack branching, and microcracking mechanisms. © 2025 Elsevier Ltd and Techna Group S.r.l.

关键词： Ceramic materials

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Julolidine functionalized benzimidazoline-doped fullerene derivatives for efficient and stable perovskite solar cells

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Interdisciplinary materials 2024年第3期3卷 369-379页

作者： Yanqing Zhu Chenglong Li JiaHui Chen Yuxi Zhang Jianfeng Lu Min Hu Wangnan Li Fuzhi Huang Yi-Bing Cheng Hyesung Park Shengqiang Xiao State Key Laboratory of Silicate Materials for Architectures Wuhan University of TechnologyWuhanChina State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhanChina School of Electronic and Electrical Engineering Hubei Province Engineering Research Centre for Intelligent Micro-Nano Medical Equipment and Key TechnologiesWuhan Textile UniversityWuhanChina Hubei Key Laboratory of Low Dimensional Optoelectronic Material and Devices Hubei University of Arts and ScienceXiangyangHubeiChina KU-KIST Graduate School of Converging Science and Technology Korea UniversitySeoulRepublic of Korea Department of Integrative Energy Engineering Korea UniversitySeoulRepublic of Korea Hubei Key Laboratory of Fuel Cell WuhanChina

Fullerene derivatives are highly attractive materials in solar cells,organic thermoelectrics,and other ***,the intrinsic low electron mobility and electrical conductivity restrict their potential device performance,such as perovskite solar cells(PSCs).Herein,we successfully enhanced the electric properties and morphology of phenyl-C61-butyric acid methyl ester(PCBM)by n-doping it with a benzimidazoline derivative,9-(1,3-dimethyl-2,3-dihydro-1H-benzoimidazol-2-yl)-julolidine(JLBI-H)via a solution *** found the n-doping can not only improve the conductivity and optimize the band alignment but also enable the PCBM to have a constantly strong charge extraction ability in a wide temperature from 173 to 373 K,which guarantees a stable photovoltaic performance of the corresponding PSCs under a wide range of operating *** the JLBI-H-doped PCBM,we improved the efficiency from 17.9%to 19.8%,along with enhanced stability of the nonencapsulated devices following the aging protocol of ISOS-D-1.

关键词： charge extraction electron mobility n-doping PSCs wide operation temperature

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